Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11981911
rs11981911
0.925 0.040 7 27848395 intron variant C/T snv 0.44
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.700 1.000 1 2018 2018
dbSNP: rs13247499
rs13247499
7 28139639 intron variant C/A snv 0.10
Alanine aminotransferase measurement
0.700 1.000 1 2018 2018
dbSNP: rs6977955
rs6977955
7 28117268 intron variant C/T snv 0.32
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2017 2017
dbSNP: rs9648346
rs9648346
1.000 0.120 7 28120494 intron variant C/A;G snv
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.700 1.000 1 2018 2018
dbSNP: rs860262
rs860262
0.807 0.200 7 28154778 intron variant C/A;T snv 0.41
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs10225163
rs10225163
0.925 0.120 7 27886026 intron variant C/G snv 0.53
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2012 2012
dbSNP: rs4722758
rs4722758
0.925 0.080 7 28116987 intron variant C/G snv 0.31
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs57585717
rs57585717
1.000 0.080 7 28109636 intron variant G/A snv 0.25
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs78823938
rs78823938
1.000 0.080 7 28101332 intron variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs481806
rs481806
7 28167681 intron variant G/T snv 0.77
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution
0.700 1.000 1 2019 2019
dbSNP: rs1029534
rs1029534
7 28149464 intron variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2013 2013
dbSNP: rs1557779
rs1557779
7 27955139 intron variant T/C snv 0.85
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1635851
rs1635851
7 28148187 intron variant C/T snv 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs1635852
rs1635852
0.882 0.160 7 28149792 intron variant T/C snv 0.42
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2009 2009
dbSNP: rs1708299
rs1708299
7 28150327 intron variant A/G snv 0.77
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2010 2010
dbSNP: rs508347
rs508347
7 28173205 intron variant T/C snv 0.69
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs552707
rs552707
7 28165684 intron variant T/C snv 0.77
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2014 2014
dbSNP: rs73091214
rs73091214
7 28160705 intron variant T/C snv 7.0E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2017 2017
dbSNP: rs849141
rs849141
0.851 0.240 7 28145472 intron variant A/G snv 0.78
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2009 2009
dbSNP: rs1635853
rs1635853
7 28149930 intron variant T/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs757138
rs757138
7 27949784 intron variant T/G snv 0.38
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2018 2018
dbSNP: rs4722758
rs4722758
0.925 0.080 7 28116987 intron variant C/G snv 0.31
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs917115
rs917115
1.000 0.080 7 28132967 intron variant T/C snv 0.41
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs860262
rs860262
0.807 0.200 7 28154778 intron variant C/A;T snv 0.41
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs10276381
rs10276381
1.000 0.040 7 28150502 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015